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NCT00775554 Clinical Trial

Comparison Study of Using Ultrasound Guidance for Hematoma Blocks vs. Traditional Approach

Forearm Fracture Clinical Trial

Official title:
"Are Ultrasound-guided Hematoma Blocks for Distal Forearm Fractures Superior to the Landmark-guided Method for Hematoma Blocks?"

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00775554
Other study ID # 08-118
Secondary ID
Status Withdrawn
Phase N/A
First received October 17, 2008
Last updated October 13, 2015
Start date September 2008

Study information
Verified date October 2008
Source St. Luke's-Roosevelt Hospital Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Will use visual analog scales to compare effectiveness of traditional hematoma block vs ultrasound guided hematoma block with regards to pain. This will be done for closed forearm fractures.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date August 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age > 18

- Closed forearm fracture

Exclusion Criteria:

- Mentally impaired, visually impaired or deaf

- Age < 18

- Alcohol on board

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Other:
• ultrasound guided hematoma block
pt. will receive ultrasound guided hematoma block
• ultrasound guided hematoma block
ultrasound will be used to guide hematoma blocks

Locations
Country Name City State
United States St. Luke's Roosevelt Hospital New York City New York

Sponsors (1)
Lead Sponsor Collaborator
St. Luke's-Roosevelt Hospital Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual analog scale movement No
See also
  Status Clinical Trial Phase
Not yet recruiting NCT05537831 - Ultrasound Guided Hematoma Block in Distal Forearm Fractures N/A
Completed NCT03906929 - Exposed Versus Buried Intramedullary K-wires for Pediatric Forearm Fractures N/A
Completed NCT03297047 - Comparing Forearm and Upper Arm Combi Cast for Distal Forearm Fractures in Children N/A
Terminated NCT00763880 - Hematoma Block as an Adjunct to Procedural Sedation for Forearm Fracture Reduction Phase 4
Recruiting NCT04941612 - Use of the Bioabsorbable Activa IM-Nail™ in Pediatric Diaphyseal Forearm Fractures N/A
Completed NCT02769117 - Bone Ultrasound to Access Fracture Healing N/A
Completed NCT00239889 - Efficacy and Safety of Salmon Calcitonin Nasal Spray in Improving Muscle Strength and Reducing Pain After Forearm Fracture in Postmenopausal Women Phase 4
Recruiting NCT04846543 - Bioresorbable Intramedullary Nailing of Forearm Fractures N/A
Completed NCT05674383 - Ultrasound Guided Axillary Nerve Block Compared to Hematoma Block in Patients With Closed Reposition of Distal Forearm Fractures N/A
Terminated NCT03097757 - Trial of Ultrasound Guidance for Reduction of Pediatric Forearm Fractures N/A
Completed NCT03474900 - Biodegradable Versus Titanium Nailing in Forearm Shaft Fractures in Children N/A
Completed NCT03377907 - Pain Alleviation of Forearm Fractures N/A
Completed NCT03805204 - Vascularity of the Ulna and Its Association With Forearm Nonunion
Completed NCT03555929 - Impact on Sensitivity and Motor Block Duration of an Intravenous Dexamethasone an Axillary Block With Mepivacaine. Phase 3
Completed NCT01567072 - Non Steroidal Antiinflammatory Drugs Influence on Heal of Distal Radius Fracture Phase 3
Recruiting NCT06381622 - Combining Lidocaine and Ropivacaine for an Infraclavicular Brachial Plexus Nerve Block Phase 3